E80.4
BillableGilbert syndrome
Gilbert syndrome
Coding Notes
Includes
Conditions included under this code
- defects of catalase and peroxidase
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
Related Codes(7)
E80.0Hereditary erythropoietic porphyria
E80.1Porphyria cutanea tarda
E80.2Other and unspecified porphyria
E80.3Defects of catalase and peroxidase
E80.5Crigler-Najjar syndrome
E80.6Other disorders of bilirubin metabolism
E80.7Disorder of bilirubin metabolism, unspecified
ICD-11 Equivalents(1)
ICD-11 Equivalents
View full mappingCorresponding ICD-11 codes from the WHO crosswalk mapping
Also Known As / Clinical Terms(143)
SNOMED CT
- Inherited disorder of bilirubin metabolism5655007
- Benign unconjugated bilirubinaemia syndrome27503000
- Benign unconjugated bilirubinemia syndrome27503000
- Cholaemia familiaris simplex27503000
- Cholemia familiaris simplex27503000
- Chronic intermittent juvenile jaundice27503000
- Congenital familial cholaemia27503000
- Congenital familial cholemia27503000
- Constitutional hepatic dysfunction27503000
- Familial nonhaemolytic bilirubinaemia27503000
- Familial nonhaemolytic jaundice27503000
- Familial nonhemolytic bilirubinemia27503000
- Familial nonhemolytic jaundice27503000
- Gilbert syndrome27503000
- Gilbert's disease27503000
- Gilbert's syndrome27503000
- Gilbert-Lereboullet syndrome27503000
- Gilberts syndrome27503000
- Hereditary nonhaemolytic jaundice27503000
- Hereditary nonhemolytic jaundice27503000
- Low-grade chronic hyperbilirubinaemia syndrome27503000
- Low-grade chronic hyperbilirubinemia syndrome27503000
- Meulengracht syndrome27503000
- Neonatal jaundice due to Gilbert syndrome206456003
- Neonatal jaundice due to Gilbert's syndrome206456003
UMLS
- Arias Type HyperbilirubinemiaC0017551
- Arias Type HyperbilirubinemiasC0017551
- Benign unconjugated bilirubinaemia syndromeC0017551
- Benign unconjugated bilirubinemia syndromeC0017551
- Cholaemia familiaris simplexC0017551
- Cholemia familiaris simplexC0017551
- Chronic intermittent juvenile jaundiceC0017551
- Congenital familial cholaemiaC0017551
- Congenital familial cholemiaC0017551
- Constitutional Liver DysfunctionC0017551
- Constitutional hepatic dysfunctionC0017551
- Constitutional liver dysfunctionC0017551
- Disease, GilbertC0017551
- Disease, Gilbert'sC0017551
- Familial Nonhemolytic JaundiceC0017551
- Familial nonhaemolytic bilirubinaemiaC0017551
- Familial nonhaemolytic jaundiceC0017551
- Familial nonhemolytic bilirubinemiaC0017551
- Familial nonhemolytic jaundiceC0017551
- GILBERT DISC0017551
- GILBERT SYNDROMEC0017551
- GILBERTS DISC0017551
- Gilbert DiseaseC0017551
- Gilbert SyndromeC0017551
- Gilbert diseaseC0017551
- Gilbert syndromeC0017551
- Gilbert's DiseaseC0017551
- Gilbert's SyndromeC0017551
- Gilbert's diseaseC0017551
- Gilbert's syndromeC0017551
- Gilbert's syndrome (disorder)C0017551
- Gilbert-Lereboullet SyndromeC0017551
- Gilbert-Lereboullet syndromeC0017551
- Gilberts DiseaseC0017551
- Gilberts SyndromeC0017551
- Gilberts syndromeC0017551
- HBLRGC0017551
- HYPERBILIRUBINEMIA IC0017551
- HYPERBILIRUBINEMIA, ARIAS TYPEC0017551
- HYPERBILIRUBINEMIA, GILBERT TYPEC0017551
- Hereditary nonhaemolytic jaundiceC0017551
- Hereditary nonhemolytic jaundiceC0017551
- Hyperbilirubinemia 1C0017551
- Hyperbilirubinemia 1sC0017551
- Hyperbilirubinemia IC0017551
- Hyperbilirubinemia, Arias TypeC0017551
- Hyperbilirubinemias, Arias TypeC0017551
- Jaundice, congenital nonhemolyticC0017551
- Low-grade chronic hyperbilirubinaemia syndromeC0017551
- Low-grade chronic hyperbilirubinemia syndromeC0017551
- Meulengracht SyndromeC0017551
- Meulengracht syndromeC0017551
- Syndrome, GilbertC0017551
- Syndrome, Gilbert'sC0017551
- Unconjugated Benign BilirubinemiaC0017551
- Unconjugated benign bilirubinemiaC0017551
- congenital nonhemolytic jaundiceC0017551
- diseases gilbertC0017551
- familial nonhemolytic jaundiceC0017551
- gilbert diseaseC0017551
- gilbert syndromeC0017551
- gilbert syndromesC0017551
- gilbert's diseaseC0017551
- gilbert's syndromeC0017551
- gilberts diseaseC0017551
- gilberts syndromeC0017551
- hereditary nonhemolytic jaundiceC0017551
- meulengracht syndromeC0017551
- syndrome gilbert'sC0017551
Clinical Terms
- Meulengracht Syndrome
- Gilbert-Lereboullet Syndrome
- gilberts disease
- Neonatal jaundice due to Gilbert syndrome
- Congenital familial cholemia
- Unconjugated benign bilirubinemia
- Gilbert Disease
- Inherited disorder of bilirubin metabolism
- Familial nonhaemolytic bilirubinaemia
- Constitutional liver dysfunction
- Gilbert's Disease
- gilbert syndromes
- Jaundice, congenital nonhemolytic
- gilberts syndrome
- Cholemia familiaris simplex
- diseases gilbert
- Disease, Gilbert's
- Chronic intermittent juvenile jaundice
- Gilbert's syndrome (disorder)
- Hyperbilirubinemia I
- familial nonhemolytic jaundice
- Gilbert's syndrome
- Disease, Gilbert
- Arias Type Hyperbilirubinemia
- Hereditary nonhaemolytic jaundice
- GILBERT DIS
- Syndrome, Gilbert's
- Constitutional hepatic dysfunction
- HYPERBILIRUBINEMIA, ARIAS TYPE
- Familial nonhaemolytic jaundice
- GILBERTS DIS
- Familial nonhemolytic bilirubinemia
- HYPERBILIRUBINEMIA, GILBERT TYPE
- Cholaemia familiaris simplex
- HBLRG
- congenital nonhemolytic jaundice
- Benign unconjugated bilirubinaemia syndrome
- Arias Type Hyperbilirubinemias
- Hyperbilirubinemia 1
- Benign unconjugated bilirubinemia syndrome
- Hyperbilirubinemia 1s
- Hereditary nonhemolytic jaundice
- Congenital familial cholaemia
- Neonatal jaundice due to Gilbert's syndrome
- Low-grade chronic hyperbilirubinaemia syndrome
- Syndrome, Gilbert
- Hyperbilirubinemias, Arias Type
- Low-grade chronic hyperbilirubinemia syndrome
- syndrome gilbert's
Frequently Asked Questions
What is the ICD-10 code for gilbert syndrome?
The ICD-10-CM code for gilbert syndrome is E80.4. The full clinical description is "Gilbert syndrome". E80.4 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code E80.4 mean?
ICD-10-CM code E80.4 represents “Gilbert syndrome”. It is classified under Chapter 4: Endocrine, Nutritional and Metabolic Diseases and is a billable/specific code that can be used on a claim.
Is E80.4 a billable code?
Yes, E80.4 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E80.4 in?
E80.4 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E80.4?
E80.4 has Excludes1 notes indicating codes that cannot be used together with it, including: transitory endocrine and metabolic disorders specific to newborn (P70-P74); androgen insensitivity syndrome (E34.5-); congenital adrenal hyperplasia (E25.0); and 3 more.
What SNOMED CT codes does E80.4 map to?
E80.4 maps to 3 SNOMED CT concepts: 27503000, 5655007, 206456003. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E80.4?
E80.4 is linked to 1 UMLS Concept Unique Identifier: C0017551. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does E80.4 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like gilbert syndrome affect a person's functioning — body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.
What is the ICD-11 equivalent of E80.4?
E80.4 maps to the ICD-11 code: 5C58.01 (Gilbert syndrome).
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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.